960化工网
Synthesis of geminal bisphosphonates via organocatalyzed enantioselective Michael additions of cyclic ketones and 4-piperidones†
Ana Maria Faísca Phillips,Maria Teresa Barros
Organic & Biomolecular Chemistry Pub Date : 09/29/2011 00:00:00 , DOI:10.1039/C1OB06473H
Abstract

A Michael addition reaction of cyclic ketones and piperidones to a vinyl phosphonate is described. The reaction, catalyzed by chiral diamines, produced geminal γ-oxobisphosphonates in high yields (up to 92%) and very high ees (up to >99%). Disubstituted ketones gave drs of up to 8 : 92. The synthesis and characterization of several new compounds with potential biological activity is described.

Graphical abstract: Synthesis of geminal bisphosphonates via organocatalyzed enantioselective Michael additions of cyclic ketones and 4-piperidones
平台客服
平台客服
平台在线客服